Kini R M, Evans H J
Department of Biochemistry, Medical College of Virginia, Virginia Commonwealth University, Richmond 23298.
Toxicon. 1989;27(6):613-35. doi: 10.1016/0041-0101(89)90013-5.
Snake venom phospholipase A2 enzymes induce a wide variety of pathological symptoms in animals, despite sharing a common catalytic activity and similar structural features with nontoxic mammalian pancreatic enzymes. A hypothetical model is described to explain how specific pharmacological effects, such as presynaptic neurotoxicity, cardiotoxicity, myotoxicity, anticoagulant and platelet effects are exhibited by venom PLA2 enzymes. The model is an effort to elucidate many controversial and contradictory observations which have previously been difficult to interpret. The essential feature of the model is the targeting of venom PLA2 enzymes to the specific tissue or cell due to their affinity towards specific proteins, rather than lipid domains. After the initial binding, PLA2 enzymes induce various pharmacological effects by mechanisms which are either dependent or independent of their enzymatic activity. The model and its predicted target proteins thus provide a new focus for toxin research.
蛇毒磷脂酶A2酶在动物体内会引发多种病理症状,尽管它们与无毒的哺乳动物胰腺酶具有共同的催化活性和相似的结构特征。本文描述了一个假设模型,以解释毒液PLA2酶如何表现出特定的药理作用,如突触前神经毒性、心脏毒性、肌肉毒性、抗凝和血小板效应。该模型旨在阐明许多以前难以解释的有争议和相互矛盾的观察结果。该模型的基本特征是,毒液PLA2酶由于对特定蛋白质而非脂质结构域具有亲和力,从而靶向特定组织或细胞。初始结合后,PLA2酶通过依赖或不依赖其酶活性的机制诱导各种药理作用。因此,该模型及其预测的靶蛋白为毒素研究提供了新的重点。